Efficacy and safety of Xuebijing combined with ulinastatin in the treatment of sepsis complicated by acute lung injury: a meta-analysis.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2026-08-15 eCollection Date: 2026-01-01 DOI:10.62347/BGCR6053
Ting Zhang, Zhenfei Yuan
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引用次数: 0

Abstract

Objective: To evaluate the efficacy and safety of Xuebijing injection combined with ulinastatin in patients with sepsis complicated by acute lung injury.

Methods: PubMed, Web of Science, the Cochrane Library, VIP Database, China National Knowledge Infrastructure and Wanfang Database were searched from inception to January 2026. Two reviewers independently screened studies, extracted data and assessed the risk of bias using the revised Cochrane Risk-of-Bias Tool for Randomized Trials, Version 2, for randomized controlled trials (RCTs) and the Risk Of Bias In Non-randomized Studies of Interventions tool for the retrospective study. Meta-analyses were performed using R version 4.2.0.

Results: Thirteen studies involving 1,158 patients (670 in the combination therapy group and 488 in the control group) were included. Compared with control therapy, Xuebijing plus ulinastatin significantly reduced TNF-α, IL-6, HMGB-1, PCT and CRP levels; improved the oxygenation index; reduced the extravascular lung water index and Acute Physiology and Chronic Health Evaluation II score and shortened mechanical ventilation duration (all P < 0.05). The total effective rate (RD 0.179, 95% CI 0.101-0.257; NNT = 5.6; P < 0.001) and 28-day survival rate (RD 0.118, 95% CI 0.002-0.234; NNT = 8.5; P = 0.047) were significantly higher in the combination group, whereas the incidence of adverse events did not differ significantly between groups (RD -0.004, 95% CI -0.049-0.042; P = 0.881). Sensitivity analyses supported the robustness of the findings.

Conclusion: Xuebijing combined with ulinastatin may reduce inflammation, improve lung function and disease severity, shorten mechanical ventilation duration and increase response and survival rates without increasing adverse events. Owing to heterogeneity in treatment regimens and inclusion criteria, these findings require validation in large-scale, multicenter RCTs.

血必净联合乌司他丁治疗脓毒症合并急性肺损伤的疗效和安全性:荟萃分析。
目的:评价血必净注射液联合乌司他丁治疗脓毒症合并急性肺损伤的疗效和安全性。方法:检索PubMed、Web of Science、Cochrane图书馆、VIP数据库、中国国家知识基础设施和万方数据库,检索时间为建库至2026年1月。两名审稿人独立筛选研究、提取数据并评估偏倚风险,使用修订后的Cochrane随机对照试验(rct)偏倚风险工具第2版和回顾性研究的非随机干预研究偏倚风险工具。meta分析采用R 4.2.0版本。结果:纳入13项研究,共1158例患者(联合治疗组670例,对照组488例)。与对照组比较,血必净联合乌司他丁显著降低TNF-α、IL-6、HMGB-1、PCT、CRP水平;提高了氧合指数;降低了血管外肺水指数和急性生理与慢性健康评价II评分,缩短了机械通气时间(均P < 0.05)。联合用药组总有效率(RD 0.179, 95% CI 0.101 ~ 0.257; NNT = 5.6, P < 0.001)和28天生存率(RD 0.118, 95% CI 0.002 ~ 0.234; NNT = 8.5, P = 0.047)显著高于联合用药组,而不良事件发生率组间无显著差异(RD -0.004, 95% CI -0.049 ~ 0.042; P = 0.881)。敏感性分析支持了研究结果的稳健性。结论:血必净联合乌司他丁可减轻炎症反应,改善肺功能和病情严重程度,缩短机械通气时间,提高反应率和生存率,且未增加不良事件。由于治疗方案和纳入标准的异质性,这些发现需要在大规模、多中心的随机对照试验中进行验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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552
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